Search Results (244)

We present a simple method for customizing the optical characteristics of gold-core, silver-shell (Au@Ag) nanoparticles through controlled morphosynthesis via a seed-mediated chemical reduction approach. By systematically adjusting the concentration of cetyltrimethylammonium chloride (CTAC), we obtained precise control over both the thickness of the Ag shell and the particle shape, transitioning from spherical nanoparticles to distinctly defined nanocubes. Bright field and high-angle annular dark-field scanning transmission electron microscopy (BF-STEM and HAADF-STEM), and energy-dispersive X-ray spectroscopy (EDS) were employed to validate the structural and compositional changes. To link morphology with optical behavior, we utilized the Mie and Maxwell–Garnett theoretical models to simulate the dielectric response of the core–shell nanostructures, showing trends that align with experimental UV-visible absorption spectra. This research presents an easy and adjustable method for modifying the plasmonic properties of Ag@Au nanoparticles by varying their shape and shell, offering opportunities for advanced applications in sensing, photonics, and nanophotonics. Full article

Background and aim. Gold nanoparticles (AuNPs) offer promising potential as nanocarriers in vaccine development due to their biocompatibility, tunable surface properties and capacity to enhance antigen presentation. This study aimed to evaluate the in vitro cytocompatibility, cellular uptake and antigen processing of carcinoembryonic antigen (CEA)-functionalized AuNPs as a nanovaccine candidate. Materials and Methods. AuNPs were synthesized by citrate reduction and subsequently functionalized with CEA through physical adsorption. Nanoparticle size, morphology, and surface charge were characterized using UV–Vis spectroscopy, dynamic light scattering (DLS), and transmission electron microscopy (TEM). Cytocompatibility was assessed via MTT assay on RAW 264.7 murine macrophages. Cellular uptake and antigen processing were evaluated using hyperspectral dark-field microscopy and fluorescence microscopy with proteasomal pathway markers. Results. The synthesized AuNPs displayed a uniform spherical morphology with a mean hydrodynamic diameter of ~50 nm and a stable zeta potential. CEA conjugation slightly altered the surface charge and spectral profile. MTT assays confirmed good cytocompatibility across tested concentrations. Hyperspectral and confocal microscopy revealed the efficient uptake of CEA-AuNPs by RAW 264.7 cells and colocalization with lysosomal compartments, suggesting successful antigen processing. Conclusions. The in vitro data support the safety and biological interaction of CEA-functionalized AuNPs with macrophages. These findings highlight their potential as a nanovaccine delivery platform and warrant further in vivo evaluation to assess immunogenicity and protective efficacy. Full article

Endotoxemia often leads to microcirculatory derangement. In six sevoflurane anaesthetized Beagle dogs, we investigated the effects of 1 mg/kg of Escherichia coli lipopolysaccharide endotoxin intravenous and blood pressure (mean arterial pressure of 65 mmHg versus 85 mmHg) on microcirculation assessed on buccal mucosa using side stream dark field microscopy. Dogs were afterwards resuscitated with fluids and noradrenaline. We investigated dose requirements of noradrenaline with or without dexmedetomidine. Microcirculatory parameters, and markers of sepsis (cardiac output, mixed venous oxygen saturation, carbon dioxide gap, and lactate) were analysed before endotoxemia, after endotoxemia, after a 30 mL/kg of Ringer’s acetate fluid bolus, and during noradrenaline +/− dexmedetomidine infusion, after a second fluid bolus, and a second time after vasopressor treatment in a cross-over fashion. Endotoxemia and mean arterial pressure had no statistically significant effect on microcirculation; however, endotoxemia resulted in a decrease in cardiac output. Dexmedetomidine neither improved microcirculation nor reduced noradrenaline requirements. Full article

The topical administration of drugs on the skin by nanovesicular systems can represent a tool to treat skin pathologies. The study of nanovesicle biodistribution after skin administration is crucial to understanding their transdermal potential. A formative study enabled us to investigate the influence of some methods in the production of nanovesicles based on phosphatidylcholine, differing in their ethanol amount. Particularly, both liposomes and ethosomes produced by different methods, i.e., microfluidics and solvent injection, were considered. The evaluation of size distribution, shape and internal morphology was performed using photon correlation spectroscopy, cryogenic electron microscopy, hyperspectral dark-field microscopy and small-angle X-ray scattering. Transmission electron microscopy was then used to observe and compare the transdermal passage of selected liposomes and ethosomes applied to human skin explants in a bioreactor. The mean diameters of nanovesicles prepared by the ethanol injection method were smaller with respect to those obtained by microfluidics, measuring roughly 140 and 230 nm, respectively. The uni- or multilamellar ultrastructure of the vesicles was influenced by the solvent injection procedure. Ultrastructural analysis of skin penetration revealed (i) the ability of intact vesicles to cross the different skin layers, with ethosomes produced by the water injection method showing greater transdermal potential and (ii) the role of ethanol as a penetration enhancer. Full article

Silver nanoparticles, with various uses in pharmacy, cosmetics, sanitation, textiles, optoelectronics, photovoltaics, etc., that are provided by worldwide industrial production, estimated to hundreds of tons annually, are finally released in the environment impacting randomly the biosphere. An alternative synthesis approach could be implemented by replacing chemical reductants of silver with natural antioxidants ensuring production and utilization sustainability with focus on environmental pollution diminishing. We synthesized silver nanoparticles by using plant extracts, aiming to offer antimicrobial products with reduced impact on the environment through sustainable green-chemistry. Fresh extracts of lemon pulp, blueberry and blackberry fruits as well as of green tea dry leaves were the sources of the natural antioxidants able to ensure ionic silver reduction and silver nanoparticle formation in the form of colloidal suspensions. The four samples were characterized by UV–Vis spectrophotometry, scanning electron microscopy, dark field optical microscopy, X-ray diffractometry, dynamic light scattering, which evidenced specific fine granularity, plasmonic features, standard crystallinity, and good stability in water suspension. Antimicrobial activity was assayed using the agar diffusion method and the bacteria kill-time technique against Staphylococcus aureus and Escherichia coli. In both cases, all silver nanoparticles revealed their adequacy for the aimed purposes, the sample synthesized with green tea showing the best efficiency, which is in concordance with its highest contents of polyphenols, flavones and best total antioxidant activity. Various applications could be safely designed based on such silver nanoparticles for sustainable chemistry development. Full article

Owing to global energy demands and climate change resulting from fossil fuel use, technologies capable of converting greenhouse gases into renewable energy resources are needed. One such technology is photocatalytic CO₂ reduction, which utilises solar energy to transform CO₂ into value-added hydrocarbons. However, the application of photocatalytic CO₂ reduction is limited by the inefficiency of existing photocatalysts. In this study, we developed a nitrogen-deficient g-C₃N₄-confined PtCu dual-atom catalyst (PtCu/V_N-C₃N₄) for photocatalytic CO₂ reduction. Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy and X-ray absorption fine structure spectroscopy confirmed the atomic-level anchoring of PtCu pairs onto the nitrogen-vacancy-rich g-C₃N₄ nanosheets. The optimised PtCu/V_N-C₃N₄ exhibited superior photocatalytic performance, with CO and CH₄ evolution rates of 13.3 µmol/g/h and 2.5 µmol/g/h, respectively, under visible-light irradiation. Mechanistic investigations revealed that CO₂ molecules were preferentially adsorbed onto the PtCu dual sites, initiating a stepwise reduction pathway. In situ diffuse reflectance infrared Fourier-transform spectroscopy identified the formation of a key intermediate (HCOO*), whereas interfacial wettability studies demonstrated efficient H₂O adsorption on PtCu sites, providing essential proton sources for CO₂ protonation. Photoelectrochemical characterisation further confirmed the enhanced charge-transfer kinetics in PtCu/V_N-C₃N₄, which were attributed to the synergistic interplay between the nitrogen vacancies and dual-atom sites. Notably, the dual-active-site architecture minimised the competitive adsorption between CO₂ and H₂O molecules, thereby optimising the surface reaction pathways. This study establishes a rational strategy for designing atomically precise dual-atom catalysts through defect engineering, achieving concurrent improvements in activity, selectivity, and charge carrier utilisation for solar-driven CO₂ conversion. Full article

A method to prepare free-standing, few-micron-thick films from a dental photopolymer resin, namely UDMA-TEGDMA in a 3:1 weight ratio, doped with gold nanorods, is presented. The method is based on a sandwich structure consisting of a 4 μm thick PVA sacrificial layer, the Au-nanorod/UDMA-TEGDMA nanocomposite layer, and glycerol, all spin-coated sequentially onto a glass slide. Glycerol serves as a cover layer to shut out oxygen during photopolymerization, while the water-soluble PVA enables the subsequent detachment of the nanocomposite film by simple immersion into a liquid bath. Layer thicknesses were controlled by profilometry, while the presence of homogeneously dispersed gold nanorods was confirmed by optical spectroscopy and dark-field optical microscopy. A total of five similar spin-coating scenarios were tested, out of which two approaches produced positive results, with final nanocomposite layer thicknesses in the 2.5–4 μm range, which is smaller than the usual thickness of the oxygen inhibition layer (OIL) commonly present in these types of resins. Optimization of these technological processes and parameters to control film thickness and consistency is discussed in detail. Full article

Pulmonary exposure to carbon nanotubes (CNTs) has been linked to a series of adverse respiratory effects in animal models, including inflammation, genotoxicity, fibrosis, and granuloma formation, the degree and characteristics of which are considered dependent upon the detailed physicochemical properties of the material as inhaled. To further explore the effect of variations in physicochemical properties on pulmonary effects, two different multi-walled CNTs (MWCNTs) were tested in vivo: a pristine MWCNT (pMWCNT) (NM-401) and a surface-modified MWCNT (MWCNT-COOH). Female Sprague–Dawley rats were whole-body exposed for 28 days to MWCNT aerosols (pMWCNT (0.5 and 1.5 mg/m³) and MWCNT-COOH (1.5 and 4.5 mg/m³)) and followed up to 1 year post-exposure. The inhalation exposures resulted in relatively low estimated lung deposition. Bronchoalveolar lavage fluid (BALF) analysis indicated inflammation levels broadly consistent with deposited dose levels. Lung histopathology indicated that both MWCNTs produced very limited toxicological effects; however, global mRNA expression levels in lung tissue and BALF cytokines indicated different characteristics for the two MWCNTs. For example, pMWCNT but not MWCNT-COOH exposure induced osteopontin production, suggestive of potential pre-fibrosis/fibrosis effects linked to the higher aspect ratio aerosol particles. This is of concern as brightfield and enhanced darkfield microscopy indicated the persistence of pMWCNT fibres in lung tissue. Full article

Color metallographic samples of H59 brass alloy have been prepared by aqua regia etching. In this paper, combined with XRD (X-ray diffraction), traditional metallographic analysis, FE-SEM (field emission scanning electron microscopy), and EBSD (electron backscattering diffraction), the effect of the color metallographic method on the microstructure characterization of the H59 brass alloy was analyzed. The experimental results showed that α phases and β phases could be distinguished clearly, and the phase morphology, distribution, and content could be expressed accurately with an average error value of 5.25% for the α phase and 4.71% for the β phase. The average error rate of the phase content characterization was 4.98% (less than 5%) with the color metallographic method. In addition, it was also found in the study that the brightness and darkness of the β phase would be related to the grain orientation, and the bright grains would correspond to the low-index surface, and the dark grains to the high-index surface. As a low-cost, fast, and efficient characterization technique, the experimental results show that color metallography (CM) could replace electron backscattering diffraction (EBSD) for the analysis of the phase composition, phase distribution, phase content, and grain orientation of brass alloys, which would provide an experimental basis for optimizing alloy properties and expanding applications. Full article

In this study, a thin film of silicon carbide (SiC) was deposited on a porous silicon (P-Si) substrate using pulsed laser deposition (PLD). The photo–electrochemical etching method with an Nd: YAG laser at 1064 nm wavelength and 900 mJ pulse energy and at a vacuum of 10⁻² mbar P-Si was utilized to create a sufficiently high amount of surface area for SiC film deposition to achieve efficient SiC film growth on the P-Si substrate. X-ray diffraction (XRD) analysis was performed on the crystalline structure of SiC and showed high-intensity peaks at the (111) and (220) planes, indicating that the substrate–film interaction is substantial. Surface roughness particle topography was examined via atomic force microscopy (AFM), and a mean diameter equal to 72.83 nm was found. Field emission scanning electron microscopy (FESEM) was used to analyze surface morphology, and the pictures show spherical nanoparticles and a mud-sponge-like shape demonstrating significant nanoscale features. Photoluminescence and UV-Vis spectroscopy were utilized to investigate the optical properties, and two emission peaks were observed for the SiC and P-Si substrates, at 590 nm and 780 nm. The SiC/P-Si heterojunction photodetector exhibited rectification behavior in its dark I–V characteristics, indicating high junction quality. The spectral responsivity of the SiC/P-Si observed a peak responsivity of 0.0096 A/W at 365 nm with detectivity of 24.5 A/W Jones, and external quantum efficiency reached 340%. The response time indicates a rise time of 0.48 s and a fall time of 0.26 s. Repeatability was assured by the tight clustering of the data points, indicating the good reproducibility and stability of the SiC/P-Si deposition process. Linearity at low light levels verifies efficient photocarrier generation and separation, whereas a reverse saturation current at high intensities points to the maximum carrier generation capability of the device. Moreover, Raman spectroscopy and energy dispersive spectroscopy (EDS) analysis confirmed the structural quality and elemental composition of the SiC/P-Si film, further attesting to the uniformity and quality of the material produced. This hybrid material’s improved optoelectronic properties, achieved by combining the stability of SiC with the quantum confinement effects of P-Si, make it useful in advanced optoelectronic applications such as UV-Vis photodetectors. Full article

This study focuses on the design of a novel electrode for an energy storage system utilizing EDEN (electrochemical-based decarbonizing energy) technology. This technology implies a chlor-alkali electrochemical cell with dual functionality: first, the electrolysis of water and NaCl to produce hydrogen (H₂) and chlorine (Cl₂), and subsequently, the utilization of these products in an H₂/Cl₂ fuel cell to generate electricity. Bimetallic RuPt nanoparticles have been synthesized on Vulcan carbon (C-V) from organometallic precursors to be used as electrocatalysts. Characterization includes transmission electron microscopy (TEM), high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), and powder X-ray diffraction (XRD). The RuPt/C-V-based electrode demonstrated notable performance in the target reversible electrochemical cell, acting as the anode for electrolysis and as the cathode in fuel-cell mode. Testing in a 3D-printed electrochemical cell revealed high efficiency, with a coulombic efficiency exceeding 96% for hydrogen production, yielding 11.75 mg·Wh⁻¹ and achieving a power output of approximately 4.5 mW·cm⁻² in H₂/Cl₂ fuel-cell operation. Full article

In the argillic alteration zone of the SinAbad area of the Urumieh–Dokhtar magmatic belt (Iran), Mg-rich, Fe-poor chlorites, which crystallised at temperatures between 160 °C and 260 °C, were affected by extensive alteration to smectite mixed-layering at the micro- and nano-scales during the retrograde evolution of the hydrothermal system. Chlorites retain their usual optical aspect and properties, except for the index of refraction perpendicular to the (001) layers, which becomes lower than those parallel to the layers, producing an increase in birefringence and change in the optic and elongation signs, in comparison to the ordinary ones for Mg chlorites. Scanning electron microscopy (SEM) maps and compositions, and electron microprobe (EMP) analyses indicate minor but ubiquitous Ca (and K) content. X-ray diffraction (XRD) of chloritic concentrates allowed the identification of chlorite and tosudite. High-resolution transmission electron microscopy (HRTEM) images show major 14 Å (chlorite), with the frequent presence of 24 Å (contracted tosudite) individual layers and small packets up to five layers thick. Lateral change from 14 Å to 24 Å individual layers has been visualised. High-resolution chemical maps obtained in high-angle annular dark-field (HAADF) mode confirm the existence of areas preferentially dominated by chlorite or tosudite. The overall chemical compositions obtained by SEM, EMP, and transmission electron microscopy (TEM) align from the chlorite to the tosudite end-members, whose pure compositions could be determined from extreme analytical electron microscopy (AEM) analyses. The described intergrowths and interlayers, under the optical resolution, could provide a clue to explain changes in the normal optic properties of chlorite, which are mentioned, but not explained, in the literature. Full article

Digital Holographic Microscopy (DHM) is a method of converting hologram images into three-dimensional (3D) images by image processing, which enables us to obtain the detailed shapes of the objects to be observed. Three-dimensional imaging of the microscopic objects by DHM can contribute to the early diagnosis and the detection of the diseases in the medical field by observing the shape of the cells. DHM requires several experimental components. One of them is the laser, which is a problem because its high power may cause the deformation and the destruction of the cells and the death of the microorganisms. Since the greatest advantage of DHM is the detailed geometrical information of the object by 3D measurement, the loss of such information is a serious problem. To solve this problem, a Neutral Density (ND) filter has been used to reduce power after the laser irradiation. However, the image acquired by the image sensor becomes too dark to obtain sufficient information, and the effect of noise increased due to the decrease in the amount of light. Therefore, in this paper, we propose the Frame-Stacking Method (FSM) for dark DHM for reproducing 3D profiles that enable us to observe the shape of the objects from the images taken in low-power environments when the power is reduced. The proposed method realizes highly accurate 3D profiles by the frame decomposition of the low-power videos into images and superimposing and rescaling the obtained low-power images. On the other hand, the continuous irradiation of the laser beam for a long period may destroy the shape of the cells and the death of the microorganisms. Therefore, we conducted experiments to investigate the relationship between the number of superimposed images corresponding to the irradiation time and the 3D profile, as well as the characteristics of the power and the 3D profile. Full article

Aluminum nanoparticles (Al NPs) are interesting for energetic and plasmonic applications due to their enhanced size-dependent properties. Passivating the surface of these particles is necessary to avoid forming a native oxide layer, which can degrade energetic and optical characteristics. This work utilized a radiofrequency (RF)-driven capacitively coupled argon/hydrogen plasma to form surface-modified Al NPs from aluminum trichloride (AlCl₃) vapor and 5% silane in argon (dilute SiH₄). Varying the power and dilute SiH₄ flow rate in the afterglow of the plasma led to the formation of varying nanoparticle morphologies: Al–SiO₂ core–shell, Si–Al₂O₃ core–shell, and Al–Si Janus particles. Scanning transmission electron microscopy with a high-angle annular dark-field detector (STEM-HAADF) and energy-dispersive X-ray spectroscopy (EDS) were employed for characterization. The surfaces of the nanoparticles and sample composition were characterized and found to be sensitive to changes in RF power input and dilute SiH₄ flow rate. This work demonstrates a tunable range of Al–SiO₂ core–shell nanoparticles where the Al-to-Si ratio could be varied by changing the plasma parameters. Thermal analysis measurements performed on plasma-synthesized Al, crystalline Si, and Al–SiO₂ samples are compared to those from a commercially available 80 nm Al nanopowder. Core–shell particles exhibit an increase in oxidation temperature from 535 °C for Al to 585 °C for Al–SiO₂. This all-gas-phase synthesis approach offers a simple preparation method to produce high-purity heterostructured Al NPs. Full article

Surface acoustic wave-based (SAW) sensors are of great interest due to their high sensibility and fast and stable responses. They can be obtained at an overall low cost and with an intuitive and easy-to-use method. The chemical sensitization of a piezoelectric transducer plays a key role in defining the properties of SAW sensors. In this study, we investigate the structural and adhesion properties of a new class of coating material based on polyurethane polymeric composites. We used dark-field microscopy (DFM) and scanning electron microscopy (SEM) to observe the microstructure of polyurethane composite coatings on piezoelectric sensor elements and to analyze the effects of the chemical resistance and adhesion test (CAT) on the coating layers obtained with the polyurethane polymeric composites. The results of the microscopy showed that all polyurethane composite coatings exhibited excellent uniformity and stability after chemical adherence testing (CAT). All of the observations were correlated with the results of the ultrasonic analysis, which demonstrated the role of polyurethane as a binder to form the stable structure of the composites and, at the same time, as an adhesion promoter, increasing the chemical resistance and the adherence of the coating layer to the complex surface of the piezoelectric sensor element. Full article